Position Details

Type Full-Time

Experience mid

Exp. Years Not specified

Education Not specified

Category Science & Research

About this role

DaVita Clinical Research (DCR) seeks a Clinical Research Coordinator to coordinate and execute late phase nephrology clinical trials in the Columbus, GA area. The role is responsible for enrollment, maintenance, close out, protocol-driven research procedures, and timely data entry and query resolution to support database lock.

Key Responsibilities

Execute clinical trials through enrollment, maintenance and close out
Perform research procedures per the study protocol
Coordinate with physician investigators and study sponsors
Enter data accurately into electronic data entry systems
Resolve data queries to meet database lock timelines

Technical Overview

Clinical research operations focused on trial execution and data quality. Includes work with electronic data entry systems for timely data entry and query resolution, under strict good clinical practice (GCP) and standard operating procedures (SOPs).

Ideal Candidate

The ideal candidate is a Clinical Research Coordinator who has coordinated and executed nephrology clinical research trials (including late phase studies) with strong GCP and protocol adherence. They are accurate with electronic data entry, responsive in resolving data queries ahead of database lock, and effective working with Principal Investigators and study sponsors.

Must-Have Skills

GCP (Good Clinical Practice) and applicable law complianceAccurate and timely data entry into the electronic data entry systemsTimely resolution of data queries to meet project timelines for database lockAccountable for successful execution of clinical trials through enrollmentmaintenance and close outCoordination of research procedures according to the study protocol

Tools & Platforms

electronic data entry systems

Required Skills

Clinical trials executionGCP compliancestudy protocol adherenceenrollmentmaintenanceclose outdata entry into electronic data entry systemsdata query resolutiondatabase lock timelinesphysician investigator coordinationSOP adherence

Hard Skills

clinical research trial executionlate phase clinical trials coordinationenrollmentmaintenanceclose outresearch procedures according to the study protocolphysician investigator collaborationdata entry into electronic data entry systemsresolution of data queriesdatabase lock supportgood clinical practice (GCP) compliancecompliance with applicable lawadherence to standard operating procedures and policies (SOPs)

Soft Skills

create an inspiring visioncollaborative environment mindsetownership of resultsinstill accountabilitystrong communicatorsrelationship buildingcompassionatepurposefulmotivated by meaningful workpositive attitudeinnovativegrowth mindset

Industry & Role

Industry Healthcare

Job Function Coordinate and manage nephrology clinical research trials in dialysis centers and physician practices with protocol and GCP compliance.

Role Subtype Clinical Research Coordinator

Keywords for Your Resume

Clinical Research CoordinatorDCRDaVita Clinical ResearchClinical Research Study CoordinatorResearch Coordinatornephrology clinical research trialsdialysis centersphysicians practiceslate phase clinical trialsenrollmentmaintenanceclose outstudy protocolphysician investigatorPrincipal InvestigatorSub-Investigatorstudy sponsorselectronic data entry systemsdata queriesdatabase lockgood clinical practiceGCPstandard operating proceduresSOPscompliance with applicable lawcolumbusgeorgiaGood Clinical Practice (GCP)data entry

Deal Breakers

Must demonstrate good clinical practice (GCP) and applicable law compliance, Must be able to perform accurate and timely data entry into electronic data entry systems, Must resolve data queries timely to meet project timelines for database lock

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Clinical Research Coordinator (DCR)

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